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7293-66-5

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7293-66-5 Usage

Description

(2-cyano-9H-fluoren-9-yl)(triphenyl)phosphonium is a phosphonium salt that features a fluorenyl group and a cyano group. It is widely recognized for its role in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. This versatile compound also finds use in the preparation of polymer materials and serves as a stabilizer in various industrial processes. The phosphonium group present in its structure endows it with utility in catalytic processes, making it a valuable asset in the fields of organic chemistry and materials science.

Uses

Used in Organic Synthesis:
(2-cyano-9H-fluoren-9-yl)(triphenyl)phosphonium is used as a reactant in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure allows for versatile reactions that contribute to the synthesis of complex organic molecules.
Used in Polymer Material Preparation:
This phosphonium salt is utilized in the preparation of polymer materials, where its properties can influence the polymer's characteristics, such as stability, reactivity, and structural integrity.
Used as an Industrial Stabilizer:
(2-cyano-9H-fluoren-9-yl)(triphenyl)phosphonium is used as a stabilizer in some industrial processes to ensure the consistency and quality of the final products.
Used in Catalytic Processes:
The presence of the phosphonium group in this chemical compound makes it useful in catalytic processes, where it can facilitate reactions and improve the efficiency of chemical transformations.
Overall, (2-cyano-9H-fluoren-9-yl)(triphenyl)phosphonium is a multifaceted chemical with applications that span across various industries and scientific disciplines, highlighting its importance in modern chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 7293-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7293-66:
(6*7)+(5*2)+(4*9)+(3*3)+(2*6)+(1*6)=115
115 % 10 = 5
So 7293-66-5 is a valid CAS Registry Number.

7293-66-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-cyano-9H-fluoren-9-yl)-triphenylphosphanium,bromide

1.2 Other means of identification

Product number -
Other names 2-Cyanfluorenyl-(9)-triphenylphosphonium-bromid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7293-66-5 SDS

7293-66-5Relevant articles and documents

A comprehensive study of substituent effects on poly(dibenzofulvene)s

Wong, Michael Y.,Leung, Louis M.

, p. 512 - 520 (2017/02/05)

We herein report the first cross comparison of 14 poly(dibenzofulvene) derivatives (13 novel examples and the parent poly(dibenzofulvene)) in order to understand how the choice of substituent affects the physical properties of this interesting class of semiconducting polymers. Electron withdrawing substituents decreased the polymerization reactivity and resulted in very low molecular-weight products. Di-substituted poly(dibenzofulvene)s were found to be much less soluble than the mono-analogues which can be explained by the Hansen solubility parameter system. Analysis based on absorption, emission and electrochemistry profiles suggests that polymer solubility is a very important factor that controls the degree of stacking present in the polymer due to synthetic issues. For the first time, the thermal analysis of the parent poly(dibenzofulvene) and its derivatives is reported and it was believed that depolymerization occurred much earlier than the melting transition. We have also demonstrated the orthogonal synthesis of dibenzofulvene monomers using three distinct routes (lithiation, oxidation and Wittig) to cope with functional group compatibility.

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